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高盐饮食和幽门螺杆菌感染协同上调长爪沙鼠胃黏膜中诱导型一氧化氮合酶和环氧化酶-2的表达。

Synergistic upregulation of inducible nitric oxide synthase and cyclooxygenase-2 in gastric mucosa of Mongolian gerbils by a high-salt diet and Helicobacter pylori infection.

作者信息

Toyoda T, Tsukamoto T, Hirano N, Mizoshita T, Kato S, Takasu S, Ban H, Tatematsu M

机构信息

Division of Oncological Pathology, Aichi Cancer Center Research Institute, Nagoya, Japan.

出版信息

Histol Histopathol. 2008 May;23(5):593-9. doi: 10.14670/HH-23.593.

Abstract

AIMS

The intake of salt and salty food is known as a risk factor for gastric cancer. We have previously demonstrated that a high-salt diet dose-dependently enhances Helicobacter pylori (H. pylori)-associated gastritis and stomach carcinogenesis in Mongolian gerbils. In this study, we focused on the influence of excessive salt intake on the expression of inflammatory mediators involved in progression of H. pylori-induced chronic gastritis.

METHODS AND RESULTS

A total of 45 stomach samples from Mongolian gerbils were evaluated by immunohistochemistry. The animals were infected with H. pylori and fed basal (0.32%) or a high-salt (10%) diet, and sacrificed after 40 weeks. Proliferative activity and expression of cyclooxygenase-2 (COX-2) in gastric mucosa were significantly increased in H. pylori-infected gerbils. The additional high-salt diet significantly up-regulated the expression of inducible nitric oxide synthase (iNOS) and COX-2 in H. pylori-infected groups (P<0.01 and P<0.05, respectively), while no significant effects were noted in non-infected animals. There was significant synergistic interaction between H. pylori infection and 10% NaCl diet on the expression of iNOS (P<0.05) and also a tendency for enhanced COX-2 expression (P=0.0599).

CONCLUSIONS

The present results suggest that a high-salt diet works synergistically with H. pylori infection to enhance iNOS and COX-2 expression in the gastric mucosa of Mongolian gerbils, and support the hypothesis that excessive salt intake may be associated with progression of H. pylori-induced gastritis.

摘要

目的

摄入盐及咸味食物是已知的胃癌风险因素。我们之前已证明,高盐饮食会剂量依赖性地加重蒙古沙鼠幽门螺杆菌(H. pylori)相关性胃炎及胃癌发生。在本研究中,我们重点关注过量盐摄入对参与幽门螺杆菌诱导的慢性胃炎进展的炎症介质表达的影响。

方法与结果

通过免疫组织化学对45份蒙古沙鼠胃样本进行评估。动物感染幽门螺杆菌后,分别给予基础(0.32%)或高盐(10%)饮食,40周后处死。幽门螺杆菌感染的沙鼠胃黏膜中的增殖活性及环氧化酶-2(COX-2)表达显著增加。额外的高盐饮食使幽门螺杆菌感染组中的诱导型一氧化氮合酶(iNOS)及COX-2表达显著上调(分别为P<0.01和P<0.05),而在未感染动物中未观察到显著影响。幽门螺杆菌感染与10% NaCl饮食在iNOS表达上存在显著的协同相互作用(P<0.05),COX-2表达也有增强趋势(P=0.0599)。

结论

目前结果表明,高盐饮食与幽门螺杆菌感染协同作用,增强蒙古沙鼠胃黏膜中iNOS及COX-2表达,并支持过量盐摄入可能与幽门螺杆菌诱导的胃炎进展相关这一假说。

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